Frankfurt Rhine-Main Metropolitan Area
Responsible for auditing of non-clinical safety studies as well as analysis of samples from clinical trials to ensure compliance with the GLP or GCP Principles, adherence to the study-plan and the Standard Operating Procedures. Since 2017 Head of Quality Assurance GLP and responsible for the local GLP test facility. Since 2019 Leader of the working group IT of the GQMA (German Quality Management Association)
Principal Investigator at Sanofi-Aventis Deutschland GmbH, Germany. Responsible for the development of LC-MS/MS assays for small molecules and peptides. Responsible for implementation and validation of several software products. Software Engineer (ARTA 1.0 and ARTA 2.0, and other tools) which are used in the GLP/GCLP environment to control and secure the electronic raw-data workflow between Analyst, Watson LIMS and NuGenesis at Sanofi-Aventis, Germany.